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SEPRACOR INC [US](7)
UNIV WASHINGTON [US](2)
SEPRACOR INC(2)
Sepracor Inc.(2)
Olney, John, W.(1)
WELLCOME FOUND(1)
OLNEY JOHN W [US](1)
FARBER NURI B [US](1)
JEVTOVIC TODOROVIC VESNA [US] (1)
WARREN TEED PRODUCTS COMPANY(1)
专利信息
Translation Company
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[药品] 包含 'Procyclidine'
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公开号
公开日
申请号
申请日
1.
WO0189448A3
2002/8/15
WO2001IB00758
2001/3/28
专利标题
:Combination of adrenergic agonist and nmda antagonist for relieving chronic pain without adverse side effects
专利权人
:
Olney, John, W.
;
A combination of two drugs from different and unrelated categories provides effective and long-lasting relief from neuropathic pain and other chronic or intractable pain. Both drugs can be taken in a painless non-invasive manner such as by means of pills or skin patches. One drug is an α2 adrenergic agonist exemplified by clonidine. These agents reduce blood pressure and have sedative-hypnotic effects; those are unwanted side effects in a chronic daily treatment for pain. The other drug is an NM...
2.
US20020068754A1
2002/6/6
US09/820080
2001/3/28
专利标题
:Combination of adrenergic agonist and aryl-cyclo-alkanolamine for relieving chronic pain without adverse side effects
专利权人
:
This invention discloses that a combination of two drugs from two different and unrelated categories provides effective and long-lasting relief from neuropathic pain. Both drugs can be taken orally in a convenient painless non-invasive manner that does not require injections. One drug is an aryl-cyclo-alkanolamine (ACAA) which has antagonist (receptor-blocking) activity at the NMDA subclass of glutamate receptors; such drugs include procyclidine biperiden and trihexyphenidyl. The other drug is a...
3.
US2002068754A1
2002/6/6
US20010820080
2001/3/28
专利标题
:Combination of adrenergic agonist and aryl-cyclo-alkanolamine for relieving chronic pain without adverse side effects
专利权人
:
This invention discloses that a combination of two drugs, from two different and unrelated categories, provides effective and long-lasting relief from neuropathic pain. Both drugs can be taken orally, in a convenient, painless, non-invasive manner that does not require injections. One drug is an aryl-cyclo-alkanolamine (ACAA) which has antagonist (receptor-blocking) activity at the NMDA subclass of glutamate receptors
4.
JP2001527038A
2001/12/25
JP20000526210
1998/12/29
专利标题
:Semiconductor device and its manufacturing method
专利权人
:
A method for treating urinary incontinence such as incontinence resulting from bladder detrusor muscle instability using enantiomerically enriched (R)-procyclidine.The method comprises administering a therapeutically effective amount of enantiomerically enriched (R)-procyclidine or a pharmaceutically acceptable salt thereof substantially free of the (S)-procyclidine enantiomer.Pharmaceutical compositions for the treatment of urinary incontinence comprising enantiomerically enriched (R)-procyclid...
5.
JP2001527039A
2001/12/25
JP20000526211
1998/12/29
专利标题
:
专利权人
:
A method for treating urinary incontinence such as incontinence resulting from bladder detrusor muscle instability using enantiomerically enriched (S)-procyclidine.The method comprises administering a therapeutically effective amount of enantiomerically enriched (S)-procyclidine or a pharmaceutically acceptable salt thereof substantially free of the (R)-procyclidine enantiomer.Pharmaceutical compositions for the treatment of urinary incontinence comprising enantiomerically enriched (S)-procyclid...
6.
WO0189448A2
2001/11/29
WO2001IB00758
2001/3/28
专利标题
:COMBINATION OF ADRENERGIC AGONIST AND NMDA ANTAGONIST FOR RELIEVING CHRONIC PAIN WITHOUT ADVERSE SIDE EFFECTS
专利权人
:
OLNEY JOHN W [US]
;
FARBER NURI B [US]
;
JEVTOVIC TODOROVIC VESNA [US]
;
A combination of two drugs, from different and unrelated categories, provides effective and long-lasting relief from neuropathic pain and other chronic or intractable pain. Both drugs can be taken in a painless non-invasive manner, such as by means of pills or skin patches. One drug is an alpha 2 adrenergic agonist, exemplified by clonidine. These agents reduce blood pressure and have sedative-hypnotic effects
7.
EP1043992A2
2000/10/18
EP19980964970
1998/12/29
专利标题
:$i(R)-PROCYCLIDINE FOR TREATING URINARY INCONTINENCE
专利权人
:
SEPRACOR INC [US]
;
8.
EP1041981A2
2000/10/11
EP19980964973
1998/12/29
专利标题
:$i(S)-PROCYCLIDINE FOR TREATING URINARY INCONTINENCE
专利权人
:
SEPRACOR INC [US]
;
9.
US6130242A
2000/10/10
US19980222132
1998/12/29
专利标题
:S-procyclidine for treating urinary incontinence
专利权人
:
SEPRACOR INC [US]
;
A method for treating urinary incontinence, such as incontinence resulting from bladder detrusor muscle instability, using enantiomerically enriched (S)-procyclidine. The method comprises administering a therapeutically effective amount of enantiomerically enriched (S)-procyclidine, or a pharmaceutically acceptable salt thereof, substantially free of the (R)-procyclidine enantiomer. Pharmaceutical compositions for the treatment of urinary incontinence comprising enantiomerically enriched (S)-pro...
10.
WO9933454A3
1999/10/21
WO1998US27708
1998/12/29
专利标题
:S-procyclidine for treating urinary incontinence
专利权人
:
Sepracor Inc.
;
A method for treating urinary incontinence such as incontinence resulting from bladder detrusor muscle instability using enantiomerically enriched (S)-procyclidine. The method comprises administering a therapeutically effective amount of enantiomerically enriched (S)-procyclidine or a pharmaceutically acceptable salt thereof substantially free of the (R)-procyclidine enantiomer. Pharmaceutical compositions for the treatment of urinary incontinence comprising enantiomerically enriched (S)-procycl...
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